- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06104722
Comparison of the Effect of Copenhagen Adduction Exercises Performed at Different Load-intensity
Comparison of the Effects of Copenhagen Adduction Exercise Performed at Different Loading Intensities on Hip Muscle Strength Development, Delayed Muscle Soreness, and Lower Extremity Physical Fitness Parameters
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The study is a single-blind randomized controlled trial including male and female adolescent taekwondo athletes (12-18 years). Evaluators will be blinded to which group are assessing.
Participants will be recruited from the local sports clubs. Club coaches will be asked to invite club players. Players interested in participating in the study will be asked to attend a meeting where the study will be explained to them. Those who were interested will then be assessed for inclusion and exclusion criteria.
Interventions:
Sports clubs are allocated to the high-intensity Copenhagen adductor exercise group (HCAE) or the low-intensity Copenhagen adduction exercise group (LCAE). Athletes in both the low-intensity and high-intensity exercise groups will perform the exercise for 8 weeks. Athletes in the HCAE group will perform the classic Copenhagen adduction exercise protocol and at LCAE group will perform the modified Copenhagen adduction exercise protocol.
Testing procedure:
The following tests will be performed before the exercise and 4th - 8th - 16th weeks after the beginning of the exercise.
The isometric and eccentric strength of the hip adductors and abductors Hip adduction flexibility Single-leg hop test Side hop test
A 10-point visual analog scale will be used to record the level of muscle soreness and rate of perceived exertion experienced after each training session.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Ezgi Unuvar-Yuksel
- Phone Number: +905078337676
- Email: unuvarezgi@gmail.com
Study Contact Backup
- Name: Özlem Ulger, proffesor
- Phone Number: +903123051576
- Email: ozlemulger@yahoo.com
Study Locations
-
-
Altındag
-
Ankara, Altındag, Turkey, 06100
- Recruiting
- Hacettepe University
-
Contact:
- Ezgi Unüvar
- Phone Number: 05078337676
- Email: unuvarezgi@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being between the ages of 12-18
- Having a minimum of 3 years of experience as a taekwondo athlete
- Not having experienced any back, hip, or groin injuries in the last 12 months
- Participating in training sessions at least 3 days a week
- Being available to attend exercise training for 8 weeks
Exclusion Criteria:
- Having had a lower extremity orthopedic injury within the last 3 months
- Having an injury related to the hip and groin region
- Reporting a pain level of 4 or higher on the visual pain scale during the adductor squeeze test and palpation of the adductor muscles
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: high intensity copenhagen adduction exercise group
Athletes in the high-intensity copenhagen adduction exercise group will perform classic copenhagen adduction exercise protocol.
|
Copenhagen adduction exercise is an eccentric strengthening protocol of hip adductors and suitable for groin injury prevention and rehabilitation.
|
|
Experimental: low intensity copenhagen adduction exercise group
Athletes in the low-intensity copenhagen adduction exercise group will perform a modified copenhagen adduction exercise protocol.
|
Copenhagen adduction exercise is an eccentric strengthening protocol of hip adductors and suitable for groin injury prevention and rehabilitation.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
hip muscle strength
Time Frame: beginning and 4th-8th-16th weeks after beginning
|
isometric and eccentric hip adductor and abductor muscle strength will assess with a hand-held dynamometer.
|
beginning and 4th-8th-16th weeks after beginning
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
lower extremity performance
Time Frame: beginning and 4th-8th-16th weeks after beginning
|
single leg hop test and side hop test
|
beginning and 4th-8th-16th weeks after beginning
|
|
hip adduction flexibility
Time Frame: beginning and 4th-8th-16th weeks after beginning
|
hip adduction range of motion will assess with a goniometer.
|
beginning and 4th-8th-16th weeks after beginning
|
|
delayed onset muscle soreness
Time Frame: immediately after each exercise session, through 8 weeks
|
delayed onset muscle soreness will assessed with visual analog scale.
|
immediately after each exercise session, through 8 weeks
|
|
rate of perceived exertion
Time Frame: immediately after each exercise session, through 8 weeks
|
rate of perceived exertion will assessed with BORG CR10 scale(Borg Rating Of Perceived Exertion).
|
immediately after each exercise session, through 8 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
exercise compliance
Time Frame: immediately after each exercise session, through 8 weeks
|
participation status of all exercise session (%)
|
immediately after each exercise session, through 8 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Hande Guney-Deniz, Prof, Hacettepe University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- copenhagentkd2023
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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